Real-Time PCR Array as a Universal Platform for the Detection of Genetically Modified Crops and Its Application in Identifying Unapproved Genetically Modified Crops in Japan
Citations Over TimeTop 10% of 2008 papers
Abstract
We developed a novel type of real-time polymerase chain reaction (PCR) array with TaqMan chemistry as a platform for the comprehensive and semiquantitative detection of genetically modified (GM) crops. Thirty primer-probe sets for the specific detection of GM lines, recombinant DNA (r-DNA) segments, endogenous reference genes, and donor organisms were synthesized, and a 96-well PCR plate was prepared with a different primer-probe in each well as the real-time PCR array. The specificity and sensitivity of the array were evaluated. A comparative analysis with the data and publicly available information on GM crops approved in Japan allowed us to assume the possibility of unapproved GM crop contamination. Furthermore, we designed a Microsoft Excel spreadsheet application, Unapproved GMO Checker version 2.01, which helps process all the data of real-time PCR arrays for the easy assumption of unapproved GM crop contamination. The spreadsheet is available free of charge at http://cse.naro.affrc.go.jp/jmano/index.html .
Related Papers
- Real-time quantitative RT-PCR for the detection of HLA-DRα mRNA expression(2006)
- Development of real-time fluorescent quantitative PCR assay for detection of PRRSV based on TaqMan probe(2012)
- Development of real-time TaqMan-quantitative RT-PCR assay for detection of porcine reproductive and respiratory syndrome virus(2006)
- Real-time Quantitative RT-PCR for the Detection of TNF-α mRNA Expression(2006)
- Comparison of TaqMan real-time RT-PCR and conventional RT-PCR assays for detecting dengue virus(2008)